Canonical Allele Identifier: CA16604816
Gene: MEGF10 HGNC NCBI

Linked Data

ClinVar Variation Id: 390811
ClinVar RCV Id: RCV000418971
dbSNP Id: rs1057523896

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.127443046G>A , CM000667.2:g.127443046G>A GRCh38
NC_000005.9:g.126778738G>A , CM000667.1:g.126778738G>A GRCh37
NC_000005.8:g.126806637G>A NCBI36
NG_032072.1:g.157283G>A
NG_032072.2:g.157283G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000503335.7:c.2411G>A MANE Select ENSP00000423354.2:p.Cys804Tyr
ENST00000274473.6:c.2411G>A ENSP00000274473.6:p.Cys804Tyr
ENST00000503335.6:c.2411G>A ENSP00000423354.2:p.Cys804Tyr
NM_001256545.1:c.2411G>A NP_001243474.1:p.Cys804Tyr
NM_032446.2:c.2411G>A NP_115822.1:p.Cys804Tyr
XM_011543692.1:c.2411G>A XP_011541994.1:p.Cys804Tyr
XM_011543693.1:c.2411G>A XP_011541995.1:p.Cys804Tyr
XM_011543694.1:c.2411G>A XP_011541996.1:p.Cys804Tyr
XM_017009987.1:c.2576G>A XP_016865476.1:p.Cys859Tyr
XM_017009988.1:c.1271G>A XP_016865477.1:p.Cys424Tyr
NM_001256545.2:c.2411G>A MANE Select NP_001243474.1:p.Cys804Tyr
NM_032446.3:c.2411G>A NP_115822.1:p.Cys804Tyr